Department of BIN Convergence Technology, Department of Polymer Nano Science and Technology and Polymer Materials Fusion Research Center, Chonbuk National University, Deokjin-gu, Jeonju, Republic of Korea.
Department of Industrial Engineering, University of Trento, Trento, Italy.
J Cell Biochem. 2020 Jul;121(7):3642-3652. doi: 10.1002/jcb.29657. Epub 2020 Feb 24.
Exosomes (EXs) are nanocarrier vesicles with 20-50 nm dimensions. They are involved in cell proliferation and differentiation and in protecting the integrity of materials. They can be isolated from plasma and immunoreactive components. Recent studies demonstrated their potential role in cartilage regeneration. To enhance their regenerative effect, molecules like microRNA (miR-140) can be loaded in EX that acts as RNA delivery systems. In this study, we combined EX with miR-140 to enhance cell differentiation by inducing membrane fusion and consequent miRNA released into the cytoplasm. The carrier RNA complex was successfully synthesized through freeze and thaw method leading to the formation of EX-containing miR-140. The EX morphology was assessed through transmission electron microscopy and their miR-140 uptake efficiency through real-time polymerase chain reaction (RT-PCR). The effects on bone marrow stem cells (BMSCs) were evaluated by in vitro cell culture. Cell adhesion and morphology were studied using a bio-scanning electron microscope and confocal laser scanning microscope. Differentiation BMSCs into chondrocytes was analyzed by RT-PCR and histology. Our results confirm the bioactive role of EX loaded with miR-140 in the differentiation of BMSCs into chondrocytes. EXs were biocompatible involving in the cartilage healing process through chromogenic differentiation of BMCS exploiting the tissue engineering route.
外泌体(EXs)是一种具有 20-50nm 尺寸的纳米载体囊泡。它们参与细胞增殖和分化,并保护物质的完整性。它们可以从血浆和免疫反应性成分中分离出来。最近的研究表明它们在软骨再生中的潜在作用。为了增强它们的再生效果,可以将分子如 microRNA(miR-140)加载到 EX 中,作为 RNA 输送系统。在这项研究中,我们通过诱导膜融合和随后的 miRNA 释放到细胞质中来结合 EX 和 miR-140 以增强细胞分化。通过冷冻和融解方法成功合成了载有 RNA 的复合物,导致形成含有 miR-140 的 EX。通过透射电子显微镜评估 EX 的形态,通过实时聚合酶链反应(RT-PCR)评估其 miR-140 摄取效率。通过体外细胞培养评估对骨髓基质细胞(BMSCs)的影响。使用生物扫描电子显微镜和共聚焦激光扫描显微镜研究细胞粘附和形态。通过 RT-PCR 和组织学分析来分析诱导 BMSCs 分化为软骨细胞的情况。我们的结果证实了负载 miR-140 的 EX 在诱导 BMSCs 分化为软骨细胞中的生物活性作用。EX 具有生物相容性,通过利用组织工程途径对 BMCS 进行显色分化,参与软骨愈合过程。